CareFusion recalls BD PYXIS MEDBANK TWR software version 3.9.1.9 for potential incorrect medication bin labeling during restocking. Affected units include specific serial numbers and model codes.
Due to software issue, there is a potential when a restock label is printed for a medication stored in automated dispensing cabinets, that the incorrect bin for the medication is printed on the label.
CareFusion recalls BD PYXIS MEDBANK TWR medication cabinets with software version 3.9.1.9 because printing restock labels may show the wrong medication bin. This could lead to incorrect medication dispensing if not fixed.
The software issue causes restock labels for medications in automated dispensing cabinets to print the incorrect bin location. This could result in medications being dispensed to the wrong storage area, potentially causing errors in medication handling.
Healthcare facilities using BD PYXIS MEDBANK TWR cabinets with the specific software version are most at risk. Patients and staff may be affected if medication errors occur due to mislabeled bins.
Check for the model code CR-6HH-2FH-2FM-P and software version 3.9.1.9. Affected units have specific serial numbers listed in the recall notice.
Verify the software version on your BD PYXIS MEDBANK TWR cabinet. If it is 3.9.1.9, it is affected.
The recall addresses a potential for incorrect medication bin labeling during restocking, which could lead to medication errors. However, the risk is low as it requires specific conditions to occur.
Check the software version on your cabinet. If it is 3.9.1.9, contact CareFusion for guidance on next steps.
Look for the model code CR-6HH-2FH-2FM-P and software version 3.9.1.9. Affected units have specific serial numbers listed in the recall notice.
We’ve drafted a message you can send CareFusion to request your refund or repair — edit it as you like.
Subject: Recall Z-2498-2024 — CareFusion CareFusion Hello, I own a CareFusion that is covered by recall Z-2498-2024 from CareFusion. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
Experiences, tips, and questions from readers. Every comment is reviewed before it appears.
No comments yet — be the first to share your experience.
The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
